The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
126102171 12610217 1 I 20160721 20160801 20160801 EXP GB-MYLANLABS-2016M1030349 MYLAN 0.00 Y 0.00000 20160731 CN GB GB

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
126102171 12610217 1 PS EPIRUBICIN EPIRUBICIN 1 UNK U U 91599
126102171 12610217 2 SS APREPITANT. APREPITANT 1 UNK U U 0
126102171 12610217 3 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 UNK U U 0
126102171 12610217 4 SS DEXAMETHASONE. DEXAMETHASONE 1 UNK U U 0
126102171 12610217 5 SS FLUOROURACIL. FLUOROURACIL 1 UNK U U 0
126102171 12610217 6 SS METOCLOPRAMIDE. METOCLOPRAMIDE 1 UNK U U 0
126102171 12610217 7 SS NEULASTA PEGFILGRASTIM 1 UNK U U 0
126102171 12610217 8 SS PALONOSETRON PALONOSETRON 1 UNK U U 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126102171 12610217 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126102171 12610217 Abdominal discomfort
126102171 12610217 Alopecia
126102171 12610217 Asthenia
126102171 12610217 Diarrhoea
126102171 12610217 Nausea
126102171 12610217 Neutropenia
126102171 12610217 Vomiting

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found